MAUDE Adverse Event Report: BECTON DICKINSON BD VENFLON PRO SAFETY 22GA 0.9MM OD 25MM L; INTRAVASCULAR CATHETER

Catalog Number 393222

Device Problem Break (1069)

Patient Problem Perforation of Vessels (2135)

Event Date 02/01/2024

Event Type  malfunction  

Manufacturer Narrative

H.3.If a device evaluation and/or device history review is completed, a supplemental report will be filed.

Event Description

It was reported that bd venflon pro safety 22ga 0.9mm od 25mm l needle broken the following information was provided by the initial reporter: i cannulated bd with a blue cannula last week and the cannula broke inside the patient's vein.The needle of the cannula split the plastic tube of the cannula.This caused no greater harm to the patient than the bursting of a vein.This quickly subsided and i cannulated another vein.When did the incident occur? during use.

Manufacturer Narrative

As no sample and no photo were returned, further investigation cannot be performed.Visual inspection and functional test were performed during production.Dhr was reviewed and no abnormality was reported.No similar quality notification was raised for the reported defect in the past 12 months.Therefore, the root cause cannot be determined.Complaint trend would be monitored and complaint will be reopened when sample is returned.

Event Description

I cannulated bd with a blue cannula last week and the cannula broke inside the patient's vein.The needle of the cannula split the plastic tube of the cannula.This caused no greater harm to the patient than the bursting of a vein.This quickly subsided and i cannulated another vein.When did the incident occur? during use.

• Brand Name: BD VENFLON PRO SAFETY 22GA 0.9MM OD 25MM L
• Type of Device: INTRAVASCULAR CATHETER
• Manufacturer (Section D): BECTON DICKINSON; 1 becton drive; franklin lakes NJ 07417
• Manufacturer (Section G): BECTON DICKINSON MEDICAL (SINGAPORE); 30 tuas avenue 2; singapore NJ 07417
• Manufacturer Contact: helen cox (mdr) ; 75 north fairway drive; vernon hills, IL 60061 ; 8473935694
• MDR Report Key: 18792502
• MDR Text Key: 337546560
• Report Number: 2243072-2024-00215
• Device Sequence Number: 1
• Product Code: FOZ
• UDI-Device Identifier: 00382903932221
• UDI-Public: (01)00382903932221
• Combination Product (y/n): N
• Reporter Country Code: FI
• PMA/PMN Number: UNK
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Company Representative
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date: 03/07/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: 393222
• Device Lot Number: 3274457
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 02/05/2024
• Initial Date FDA Received: 02/27/2024
• Supplement Dates Manufacturer Received: 03/07/2024
• Supplement Dates FDA Received: 03/07/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 10/15/2023
• Is the Device Single Use?: Yes
• Type of Device Usage: Initial
• Patient Sequence Number: 1